Study Start-Up Project Manager; Cincinnati

Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time,
Global Study Start‑Up Project Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace.

• Competitive bonus program
• Sign‑on/relocation bonus
• Equity awards

Position is office‑based in Cincinnati, OH.

• Efficiently manage successful execution of global start‑up, maintenance, and close‑out studies;
• Effectively lead others in a matrix environment;
• Perform quality checks on submission documents and site essential documents;
• Prepare and approve informed consent forms;
• Serve as a Sponsor point of contact for start‑up and regulatory submissions items;
• Review pertinent regulations to develop proactive solutions to start‑up challenges;
• Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits;
• Contribute to the growth and development of departmental staff, processes and systems.

• Bachelor’s degree required, advanced degree in Life Sciences preferred
• Experience with Cardiovascular and Metabolic indications in an academic and/or clinical trial setting is desired (e.g., NASH, diabetes, medical devices, coronary artery diseases)
• 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start‑Up
• Project management experience and demonstrated role in developing others
• Strong oral and written communication skills required

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